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FDA 510(k) Applications Submitted by NEIL ANDERSON, RAC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980174
01/20/1998
DUREX COLORS AND SCENTS
LONDON INTL. LLC.
K980204
01/20/1998
DUREX LATEX CONDOMS
LONDON INTL. LLC.
K160234
02/01/2016
OVENT
OVENTUS MANUFACTURING PTY LTD
K960590
02/12/1996
TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE
ALADAN CORP.
K980785
03/02/1998
STERILE, POWDERFREE LATEX EXAMINATION GLOVE
LONDON INTL. LLC.
K080606
03/04/2008
ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE
ALATECH HEALTHCARE, LLC.
K970924
03/07/1997
REGENT BIOGEL SURGICAL GLOVE, BIOGEL M GLOVE
REGENT MEDICAL
K980942
03/12/1998
REGENT BIOGEL INDICATOR INNER SURGICAL GLOVE
LONDON INTERNATIONAL GROUP, INC.
K971514
04/25/1997
REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE
LONDON INTERNATIONAL GROUP, INC.
K982924
08/20/1998
DUREX SENSIDOM LATEX CONDOM
LONDON INTL. LLC.
K082529
09/02/2008
ALATECH CHAMPION VYTEX LUBRICATED MALE LATEX CONDOM
ALATECH HEALTHCARE, LLC.
K983380
09/25/1998
DUREX LUBRAGEL LATEX CONDOM
LONDON INTL. LLC.
K984249
11/30/1998
SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE
LONDON INTERNATIONAL GROUP, INC.
K083761
12/18/2008
ALATECH POWDER FREE LATEX EXAMINATION GLOVE
ALATECH HEALTHCARE, LLC.
K980319
01/27/1998
DUREX ULTRA COMFORT
LONDON INTL. LLC.
K980516
02/10/1998
REGENT BIOGEL ORTHOPEDIC SURGICAL GLOVE
LONDON INTERNATIONAL GROUP, INC.
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